A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv408n21



Internal ID22766600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13704939..13721779hg38UCSC Ensembl
chr7:13744564..13761404hg19UCSC Ensembl
chr7:13711089..13727929hg18UCSC Ensembl
chr7:13517804..13534644hg17UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3816841
hg1916841
hg1816841
hg1716841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519178, nsv521886
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv408n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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